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PRODUCT DETAIL

Arexvy prášok a suspenzia na injekčnú suspenziu

Code 3790E
MA number EU/1/23/1740/002
Product Form: plv inu 10x120 µg+10x0,5 ml susp. (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Shelf life: 24
Container: glass vial
Route of admin.: Intramuscular use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 06.06.2023
Validity: 06.06.2028
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 19.06.2023
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